Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g12500 | A06 | 6305821 | C | T | missense_variant | MODERATE | c.1330G>A|p.Ala444Thr |
S183 S198 |
2 | BAA06g12500 | A06 | 6306809 | C | T | missense_variant | MODERATE | c.932G>A|p.Arg311Lys |
S155 S211 |
3 | BAA06g12500 | A06 | 6306912 | G | A | missense_variant | MODERATE | c.829C>T|p.Pro277Ser |
S63 |
4 | BAA06g12500 | A06 | 6307999 | C | T | missense_variant | MODERATE | c.689G>A|p.Ser230Asn |
S215 |
5 | BAA06g12500 | A06 | 6308871 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.151-1G>A| |
S36 |
6 | BAA06g12500 | A06 | 6309185 | C | T | synonymous_variant | LOW | c.75G>A|p.Pro25Pro |
S157 |
7 | BAA06g12500 | A06 | 6309221 | C | T | synonymous_variant | LOW | c.39G>A|p.Gln13Gln |
S96 |
8 | BAA06g12500 | A06 | 6314076 | C | T | upstream_gene_variant | MODIFIER | c.-4817G>A| |
S103 |